Literature DB >> 17036030

Gastroschisis in the United States 1988-2003: analysis and risk categorization of 4344 patients.

F Abdullah1, M A Arnold, R Nabaweesi, A C Fischer, P M Colombani, K D Anderson, H Lau, D C Chang.   

Abstract

OBJECTIVE: Gastroschisis is a rare congenital abdominal wall defect through which intraabdominal organs herniate and it requires surgical management soon after birth. The objectives of this study were to profile patient characteristics of this anomaly utilizing data from two large national databases and to validate previous risk stratification categories of infants born with this condition.
METHODS: An analysis was performed using 13 years of the National Inpatient Sample database (1988-1996, 1998, 1999, 2001, 2002) and 3 years of the Kids' Inpatient Database (1997, 2000, 2003). These combined databases contain information from nearly 93 million discharges in the United States. Infants with gastroschisis were identified by International Classification of Disease-9 procedure code 54.71 (repair of gastroschisis) and an age at admission of <8 days. Variables of gender, race, geographic region, co-existing diagnoses, length of stay, hospital charges adjusted to 2005 dollars, complications and inpatient mortality were collected from the databases. Infants were divided into simple and complex categories based on the absence or presence of intestinal atresia, stenosis, perforation, necrosis or volvulus. Comparisons between groups were performed using Pearson's chi (2) for categorical outcomes and the Kruskal-Wallis test for non-normally distributed continuous variables.
RESULTS: A total of 4344 infants with gastroschisis were identified. These were comprised of 44.0% female infants (n=1910), 46.4% male infants (n=2017) whereas 9.6% were not reported (n=415). Racial analysis showed the largest subset being white in 40.9% of infants (n=1775) with Hispanic infants being the next highest group reported at 17.2% (n=745). Co-existing intestinal anomalies were the most common, affecting 9.9% (n=429) infants, whereas certain cardiac (6.8%, n=294) and pulmonary (1.7%, n=72) conditions were also identified. Simple gastroschisis represented 89.1% (n=3870) of the group whereas 10.9% (n=474) were complex in nature. Simple and complex patients differed in median length of stay (28 vs 67 days, P<0.01), inpatient mortality (2.9 vs 8.7%, P<0.01) and median inflation-adjusted hospital charges (90,788 dollars vs 197,871 dollars, P<0.01).
CONCLUSIONS: These data represent a national analysis of the largest group of infants with gastroschisis to date which further aids the characterization and understanding of this serious congenital condition.

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Year:  2006        PMID: 17036030     DOI: 10.1038/sj.jp.7211616

Source DB:  PubMed          Journal:  J Perinatol        ISSN: 0743-8346            Impact factor:   2.521


  23 in total

Review 1.  Clinical risk factors for gastroschisis and omphalocele in humans: a review of the literature.

Authors:  Polina Frolov; Jasem Alali; Michael D Klein
Journal:  Pediatr Surg Int       Date:  2010-08-31       Impact factor: 1.827

2.  Risk stratification in gastroschisis: can prenatal evaluation or early postnatal factors predict outcome?

Authors:  Ryan P Davis; Marjorie C Treadwell; Robert A Drongowski; Daniel H Teitelbaum; George B Mychaliska
Journal:  Pediatr Surg Int       Date:  2009-03-10       Impact factor: 1.827

3.  Trends in incidence and outcomes of gastroschisis in the United States: analysis of the national inpatient sample 2010-2014.

Authors:  Parth Bhatt; Anusha Lekshminarayanan; Keyur Donda; Fredrick Dapaah-Siakwan; Badal Thakkar; Sumesh Parat; Shilpi Chabra; Zeenia Billimoria
Journal:  Pediatr Surg Int       Date:  2018-07-28       Impact factor: 1.827

4.  Intestinal atresia in association with gastroschisis: a 26-year review.

Authors:  Rania Kronfli; Timothy J Bradnock; Atul Sabharwal
Journal:  Pediatr Surg Int       Date:  2010-07-30       Impact factor: 1.827

5.  Gastroschisis-related complications requiring further surgical interventions.

Authors:  Florian Friedmacher; Andras Hock; Christoph Castellani; Alexander Avian; Michael E Höllwarth
Journal:  Pediatr Surg Int       Date:  2014-04-16       Impact factor: 1.827

Review 6.  A clinical-pathogenetic approach on associated anomalies and chromosomal defects supports novel candidate critical regions and genes for gastroschisis.

Authors:  Victor M Salinas-Torres; Rafael A Salinas-Torres; Ricardo M Cerda-Flores; Hugo L Gallardo-Blanco; Laura E Martínez-de-Villarreal
Journal:  Pediatr Surg Int       Date:  2018-08-09       Impact factor: 1.827

7.  Anterior Abdominal Wall Defects, Diaphragmatic Hernia, and Other Major Congenital Malformations of the Musculoskeletal System in Barbados, 1993-2012.

Authors:  Keerti Singh; Alok Kumar
Journal:  J Pediatr Genet       Date:  2017-02-13

8.  Primary fascial closure versus staged closure with silo in patients with gastroschisis: a meta-analysis.

Authors:  Sarah N Kunz; Joel S Tieder; Kathryn Whitlock; J Craig Jackson; Jeffrey R Avansino
Journal:  J Pediatr Surg       Date:  2013-04       Impact factor: 2.545

9.  Gastroschisis: preterm or term delivery?

Authors:  Henrique Soares; Ana Silva; Gustavo Rocha; Susana Pissarra; Jorge Correia-Pinto; Hercília Guimarães
Journal:  Clinics (Sao Paulo)       Date:  2010-02       Impact factor: 2.365

10.  Outcomes in neonates with gastroschisis in U.S. children's hospitals.

Authors:  Oliver B Lao; Cindy Larison; Michelle M Garrison; John H T Waldhausen; Adam B Goldin
Journal:  Am J Perinatol       Date:  2009-10-28       Impact factor: 1.862

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